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Standards Ontologies Notations
hypertrophic cardiomyopathy 7

Summary
Synonym
  • CMH7
  • cardiomyopathy, familial hypertrophic 7
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4.
Super Class
familial hypertrophic cardiomyopathy
Disease Ontology
DOID:0110313
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7137 TNNI3 troponin I3, cardiac type
Displaying 1 entry
Gene ID Gene Symbol Description Source
21954 Tnni3 troponin I, cardiac 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
29248 Tnni3 troponin I3, cardiac type
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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024